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Genetics of rare autoimmune diseases

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Genetics of rare autoimmune diseases/ edited by Javier Martin, Francisco David Carmona.
other author:	Martin, Javier.
Published:	Cham :Springer International Publishing : : 2019.,
Description:	viii, 240 p. :ill., digital ; : 24 cm.;
Contained By:	Springer eBooks
Subject:	Autoimmune diseases - Genetic aspects. -
Online resource:	https://doi.org/10.1007/978-3-030-03934-9
ISBN:	9783030039349

Genetics of rare autoimmune diseases
Genetics of rare autoimmune diseases[electronic resource] /edited by Javier Martin, Francisco David Carmona. - Cham :Springer International Publishing :2019. - viii, 240 p. :ill., digital ;24 cm. - Rare diseases of the immune system,2282-6505. - Rare diseases of the immune system..

The main aim of this volume is to provide an updated overview of the genetic basis of a group of complex disorders that are considered rare individually, but show a relatively high prevalence on the whole in developed countries: the rare autoimmune diseases. These are chronic disorders that involve long and expensive treatments with considerable side effects that may dramatically reduce the quality of life of affected people. Therefore, shedding light into their pathologic mechanisms is a major concern given their growing social and economic awareness and impact. General sections include different chapters on single entities as systemic lupus and sclerosis, Behcet's disease, Sjogren's syndrome and polymiositis, and sections devoted to autoimmune vasculitis, hepatic autoimmune conditions, as well as those affecting the nervous system, and a concluding chapter in which the shared predisposition amongst all diseases is discussed. All the chapters are given a homogeneous scheme in which the authors explain the clinical singularities of every disease and report the recent breakthrough discoveries related to them, giving a critical interpretation and suggesting future perspectives. All contributors are renowned researchers with high expertise in each disease. Due to the exponential increase in our understanding of the genetic causes of these complex diseases, a major advance in biomedical discovery is taking place. However, most of the achievements in this field are very recent and there is a lack of bibliography gathering them together. This book is thus filling a gap and will prove a useful companion to clinicians in the first place (internists, rheumatologists, clinical immunologists, and hematologists) but also to basic and applied researchers.

ISBN: 9783030039349

Standard No.: 10.1007/978-3-030-03934-9doiSubjects--Topical Terms:

795965
Autoimmune diseases
--Genetic aspects.

LC Class. No.: RC600 / .G464 2019

Dewey Class. No.: 616.723

Genetics of rare autoimmune diseases
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520 $a The main aim of this volume is to provide an updated overview of the genetic basis of a group of complex disorders that are considered rare individually, but show a relatively high prevalence on the whole in developed countries: the rare autoimmune diseases. These are chronic disorders that involve long and expensive treatments with considerable side effects that may dramatically reduce the quality of life of affected people. Therefore, shedding light into their pathologic mechanisms is a major concern given their growing social and economic awareness and impact. General sections include different chapters on single entities as systemic lupus and sclerosis, Behcet's disease, Sjogren's syndrome and polymiositis, and sections devoted to autoimmune vasculitis, hepatic autoimmune conditions, as well as those affecting the nervous system, and a concluding chapter in which the shared predisposition amongst all diseases is discussed. All the chapters are given a homogeneous scheme in which the authors explain the clinical singularities of every disease and report the recent breakthrough discoveries related to them, giving a critical interpretation and suggesting future perspectives. All contributors are renowned researchers with high expertise in each disease. Due to the exponential increase in our understanding of the genetic causes of these complex diseases, a major advance in biomedical discovery is taking place. However, most of the achievements in this field are very recent and there is a lack of bibliography gathering them together. This book is thus filling a gap and will prove a useful companion to clinicians in the first place (internists, rheumatologists, clinical immunologists, and hematologists) but also to basic and applied researchers.
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